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Tri-o-tolylphosphine → HCID 22132398, Verbindung

HRID 1856685
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1856685
C1(C)C=CC=CC=1P(C1C=CC=CC=1C)C1C=CC=CC=1C.[CH2:23]1[CH2:32][O:31][C:30]2[CH:29]=[CH:28][C:27](Br)=[CH:26][C:25]=2[O:24]1.[N:34]1[CH:39]=[CH:38][CH:37]=[C:36]([CH2:40][CH2:41][CH:42]([OH:45])[CH:43]=[CH2:44])[CH:35]=1>C(N(CC)CC)C.C(#N)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[O:31]1[C:30]2[CH:29]=[CH:28][C:27]([CH2:44][CH2:43][C:42](=[O:45])[CH2:41][CH2:40][C:36]3[CH:35]=[N:34][CH:39]=[CH:38][CH:37]=3)=[CH:26][C:25]=2[O:24][CH2:23][CH2:32]1.[O:31]1[C:30]2[CH:29]=[CH:28][C:27](/[CH:44]=[CH:43]/[CH:42]([OH:45])[CH2:41][CH2:40][C:36]3[CH:35]=[N:34][CH:39]=[CH:38][CH:37]=3)=[CH:26][C:25]=2[O:24][CH2:23][CH2:32]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 3

HCID 80271Tri-o-tolylphosphineHCID 1041416-Bromo-1,4-benzodioxaneHCID 17866850HCID 17866850, Verbindung

Produkt 2

HCID 22132398HCID 22132398, VerbindungHCID 22132429HCID 22132429, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 167845
palladium(II) acetate
Katalysator
HCID 6342AcetonitrileLösungsmittel
HCID 8471TriethylamineLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

A mixture of palladium(II) acetate (0.112 g), tri-o-tolylphosphine (0.304 g), 3,4-ethylenedioxybromobenzene (1.075 g) and (±)-5-(pyridin-3-yl)-1-penten-3-ol (0.815 g, Example 1a)) in triethylamine (10 ml) in acetonitrile (30 ml) was heated at 80° C. for 3 hours and 30 minutes. The mixture was cooled to room temperature and filtered through Celite® and the filtrate concentrated under reduced pressure. The residue was redissolved in ethyl acetate and the solution washed with water then dried over anhydrous magnesium sulfate. The solution was then filtered and concentrated under reduced pressure. The residue was purified by column chromatography over silica eluting with hexane:acetone (3:1) then (2:1) to give firstly 1-(benzo-1,4-dioxan-6-yl)-5-(pyridin-3-yl)-3-pentanone as an oil (0.812 g) and secondly (±)-trans-1-(benzo-1,4-dioxan-6-yl)-5-(pyridin-3-yl)-pent-1-en-3-ol as an oil (0.252 g).

Aufarbeitung

  1. temperatureThe mixture was cooled to room temperature
  2. filtrationfiltered through Celite®
  3. concentrationthe filtrate concentrated under reduced pressure
  4. dissolutionThe residue was redissolved in ethyl acetate
  5. washthe solution washed with water
  6. dry with materialthen dried over anhydrous magnesium sulfate
  7. filtrationThe solution was then filtered
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified by column chromatography over silica eluting with hexane:acetone (3:1)

Quellen und Nachweise

ORD-Eintrag
ord-29f913015d1e467fabab1b28a67e44cd
Quelldatensatz
uspto-grants-2000_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06143751

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